James Crowe
Faculty Member
Last active: 3/31/2019

Low expression of the interleukin (IL)-4 receptor alpha chain and reduced signalling via the IL-4 receptor complex in human neonatal B cells.

Tian C, Kron GK, Dischert KM, Higginbotham JN, Crowe JE
Immunology. 2006 119 (1): 54-62

PMID: 16764687 · PMCID: PMC1782340 · DOI:10.1111/j.1365-2567.2006.02405.x

Diminished neonatal antibody responses following infection or immunization may stem in part from intrinsic characteristics of neonatal B cells. In this study, we used B-cell subset sorting combined with gene expression assays to investigate major differences in the expression of host genes in neonatal and adult naïve B cells. We discovered significantly reduced expression of the interleukin (IL)-4 receptor alpha chain and reduced IL-4-induced signalling in neonatal B cells. Neonatal naïve B cells were susceptible to more rapid and more profound levels of apoptosis when cultured in vitro. They also exhibited a limited response to IL-4 treatment compared with adult cells. The expression level of the IL-13 receptor alpha 1 chain, a key component of the IL-13 receptor/IL-4 type II receptor, and the response to IL-13 treatment for protection against apoptosis in neonatal B cells were similar to those of the adult B cells. These studies suggest a possible mechanism underlying the limited magnitude and durability of neonatal antibody responses.

MeSH Terms (18)

Adult Analysis of Variance Apoptosis B-Lymphocytes Cell Separation Fetal Blood Flow Cytometry Gene Expression Humans Infant, Newborn Interleukin-4 Interleukin-4 Receptor alpha Subunit Interleukin-13 Interleukin-13 Receptor alpha1 Subunit Phosphorylation Reverse Transcriptase Polymerase Chain Reaction Signal Transduction STAT6 Transcription Factor

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